HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → 7-bromo-2-chloro-5-trityl-5H-pyrrolo[3,2-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-Bromo-2-chloro-5H-pyrrolo[3,2-d]pyrimidine | HCID 86731161 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-bromo-2-chloro-5-trityl-5H-pyrrolo[3,2-d]pyrimidine | HCID 86731163 | 100.3% |
Reaction Steps
A suspension of NaH (300 mg, 60% in mineral oil, 7.5 mmol) in THF (30 mL) was added a solution of 7-bromo-2-chloro-5H-pyrrolo[3,2-d]pyrimidine (1.16 g, 5.0 mmol) in THF (20 mL) dropwise at 0° C. After 20 min, a solution of TrCl (1.674 g, 6 mmol) in THF (10 mL) was added dropwise. The reaction mixture was stirred for 6 hours, quenched with brine and extracted with EtOAc (3×). The combined organic layer was dried (MgSO4), filtered and concentrated. The residue was purified by ISCO to provide the desired product (2.38 g, >99%). 1H NMR (400 MHz, CD3OD) δ 7.63 (s, 1H), 7.57 (s, 1H), 7.37-7.32 (m, 9H), 7.14-7.11 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273056B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-ffa37e89122a4380bab2baeeb457dbe2 |
| Source note | uspto-grants-2016_03 |